Fracture fixation device

ABSTRACT

Assemblies for securing fractured bone are provided. The assembly includes a first fixation element, a second fixation element, and an adjustable flexible member construct. The first fixation element having a male or a female sleeve is secured within a first portion of the fractured bone. The second fixation element having the other of the male or female sleeve telescopically received within the one of the male or female sleeve is secured within a second portion of the fractured bone. The adjustable flexible member construct extends between the first and second fixation elements and has at least one adjustable loop coupled to the first fixation element and the second fixation element and a pair of adjusting ends extending through an opening in the first fixation element. The pair of adjusting ends can be pulled to reduce a diameter of the adjustable loop and to compress fragments of the fractured bone.

CROSS-RELATED APPLICATIONS

This application is a continuation application of U.S. patent application Ser. No. 14/215,550, filed Mar. 17, 2014, now issued as U.S. Pat. No. 9,788,876 issued on Oct. 17, 2017, which application is a divisional of U.S. patent application Ser. No. 13/269,097 filed on Oct. 7, 2011, now issued as U.S. Pat. No. 8,672,969 issued on Mar. 18, 2014, which is a continuation-in-part of U.S. patent application Ser. No. 12/938,902 filed on Nov. 3, 2010, now U.S. Pat. No. 8,597,327 issued on Dec. 3, 2013, which is a continuation-in-part of U.S. patent application Ser. No. 12/489,168 filed on Jun. 22, 2009, now U.S. Pat. No. 8,361,113 issued on Jan. 29, 2013, which is a continuation-in-part of U.S. patent application Ser. No. 12/474,802 filed on May 29, 2009, now U.S. Pat. No. 8,088,130 issued on Jan. 3, 2012, which is a continuation-in-part of (a) U.S. patent application Ser. No. 12/196,405 filed on Aug. 22, 2008, now U.S. Pat. No. 8,128,658 issued on Mar. 6, 2012; (b) U.S. patent application Ser. No. 12/196,407 filed on Aug. 22, 2008, now U.S. Pat. No. 8,137,382 issued on Mar. 20, 2012; (c) U.S. patent application Ser. No. 12/196,410 filed on Aug. 22, 2008, now U.S. Pat. No. 8,118,836 issued on Feb. 21, 2012; and (d) a continuation-in-part of U.S. patent application Ser. No. 11/541,506 filed on Sep. 29, 2006, now U.S. Pat. No. 7,601,165 issued on Oct. 13, 2009.

This application is a continuation application of U.S. patent application Ser. No. 14/215,550, filed Mar. 17, 2014, now issued as U.S. Pat. No. 9,788,876 issued on Oct. 17, 2017 which application is a divisional of U.S. patent application Ser. No. 13/269,097 filed on Oct. 7, 2011, now issued as U.S. Pat. No. 8,672,969 issued on Mar. 18, 2014, which is a continuation-in-part of U.S. patent application Ser. No. 12/570,854 filed on Sep. 30, 2009, now U.S. Pat. No. 8,303,604 issued on Nov. 6, 2012, which is a continuation-in-part of U.S. patent application Ser. No. 12/014,399 filed on Jan. 15, 2008, now U.S. Pat. No. 7,909,851 issued on Mar. 22, 2011.

This application is a continuation application of U.S. patent application Ser. No. 14/215,550, filed Mar. 17, 2014, now issued as U.S. Pat. No. 9,788,876 issued on Oct. 17, 2017, which application is a divisional of U.S. patent application Ser. No. 13/269,097 filed on Oct. 7, 2011, now issued as U.S. Pat. No. 8,672,969 issued on Mar. 18, 2014, which is a continuation-in-part of U.S. patent application Ser. No. 12/702,067 filed on Feb. 8, 2010, which is a continuation of U.S. patent application Ser. No. 11/541,505 filed on Sep. 29, 2006, now U.S. Pat. No. 7,658,751 issued on Feb. 9, 2010.

This application is a continuation application of U.S. patent application Ser. No. 14/215,550, filed Mar. 17, 2014, now issued as U.S. Pat. No. 9,788,876 issued on Oct. 17, 2017, which application is a divisional of U.S. patent application Ser. No. 13/269,097 filed on Oct. 7, 2011, now issued as U.S. Pat. No. 8,672,969 issued on Mar. 18, 2014, which is a continuation-in-part of U.S. patent application Ser. No. 12/196,398 filed Aug. 22, 2008, now U.S. Pat. No. 7,959,650 issued on Jun. 14, 2011, which is a continuation-in-part of U.S. patent application Ser. No. 11/784,821 filed Apr. 10, 2007.

The disclosures of all the above applications are incorporated by reference herein.

FIELD

The present disclosure relates to devices and methods for fracture fixation, and more particularly to holding bone fragments together to permit healing.

BACKGROUND

The statements in this section merely provide background information related to the present disclosure and may not constitute prior art.

After trauma or surgical intervention, there may be a need to fix bone fragments together to immobilize the fragments and permit healing. Compressive force can be applied to the bone fragments by encircling the bone fragments or bridging the fragments together across a broken or otherwise compromised portion of the bone. The compressive forces should be applied such that upon growth of new bone, the fragments will heal together and restore strength to the trauma or surgical intervention site.

Accordingly, there is a need for apparatus and methods to apply compressive force to a bone to affect healing. Further, there is a need for an apparatus and related methods which are easy to use intraoperatively to accommodate various bone sizes, shapes, or locations of fractures.

SUMMARY

In various embodiments, the present teachings provide an assembly for securing a fractured bone. The assembly includes a first fixation element, a second fixation element, and an adjustable flexible member construct. The first fixation element is secured within a first portion of the fractured bone and has one of a male or a female sleeve extending within the fractured bone. The second fixation element is secured within a second portion of the fractured bone and has the other of the male or female sleeve extending within the fractured bone. The one of the male or female sleeve is telescopically received within the other of the male or female sleeve of the first fixation element. The adjustable flexible member construct extends between the first and second fixation elements and has at least one adjustable loop coupled to the first fixation element and the second fixation element, and a pair of adjusting ends extending through an opening in the first fixation element. The pair of adjusting ends can be pulled to reduce a diameter of the adjustable loop and to compress fragments of the fractured bone.

Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.

DRAWINGS

The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.

FIG. 1 depicts an assembly having a closed flexible member holder and an open flexible member holder according to the present teachings;

FIG. 2 depicts a frame having two open flexible member holders and an adjustable flexible member construct according to the present teachings;

FIG. 3 depicts an elongated frame according to the present teachings;

FIG. 4 depicts an elongated frame having a plurality of flexible member holders according to the present teachings;

FIGS. 5A through 5C depict frames defining openings to receive fasteners according to the present teachings;

FIGS. 6A and 6B depict adjustable flexible member constructs according to the present teachings;

FIG. 7 depicts an assembly compressing a fractured or weakened bone according to the present teachings;

FIG. 8 depicts an assembly compressing a fractured or weakened bone according to the present teachings;

FIG. 9 depicts an assembly compressing a fractured or weakened bone according to the present teachings;

FIGS. 10A and 10B depict a frame having a post extending therefrom according to the present teachings;

FIG. 11 depicts a frame having a post extending therefrom used in an assembly according to the present teachings;

FIG. 12 depicts a frame having a post extending therefrom where the frame defines a plurality of openings to receive at least one fastener according to the present teachings;

FIG. 13 depicts a side view of a surgical method according to the present teachings;

FIG. 14 depicts a top view of a surgical method according to the present teachings;

FIGS. 15A-15D depict side views of fixation of a fracture in surgical methods according to the present teachings;

FIGS. 15E and 15F depict a section view of the screw assembly of FIG. 15D;

FIGS. 16A and 16B depict a spinal repair using apparatus according to the present teachings; and

FIGS. 17A-17D depict a bone repair using the screw assembly of FIG. 15D.

DETAILED DESCRIPTION

The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features. While the present disclosure relates to fracture fixation, the apparatus and methods of the present teachings can be used with other orthopedic and non-orthopedic procedures as well.

Referring to FIGS. 1 and 2, an assembly 10 is provided according to various embodiments of the present teachings. The assembly 10 includes a frame 12 and an adjustable flexible member construct 14. As further detailed below and as depicted in FIG. 7, regions of the adjustable flexible member construct 14 are partially disposed in the frame 12 such that the adjustable flexible member construct 14 and the frame encircle a bone 16 having fragments 18 and 18′ due to surgical intervention, injury, or disease. While the present disclosure may exemplify a fractured bone, it is understood that any of the reasons for bone compromise may be used with the present teachings. It is further understood that the frame 12 can be used in connection with other frames that are placed on a different or opposing face of the bone 16. The various embodiments disclosed herein can also be used to stabilize other implants, such as those used in revision surgery or for oncological purposes.

In various embodiments, the assembly 10, assembly 110, 210 as detailed later herein, or the adjustable flexible member construct 14 alone is used to compresses the respective fragments together and to affect healing at the compromised bone 16. Bones suitable for use with the present teachings include any bone in the body, such as the vertebrae, long bones of the arms, legs or fingers; curved bones, such as the ribs; flat bones, such as those of the wrist or feet, for example, and the like. Any bones of the legs, arms, torso, hands, feet, head, are suitable for use with the apparatus and methods of the present teachings.

Referring to FIGS. 1 through 5C, the frame 12 includes a lower surface 20, an upper surface 22, and at least flexible member holders 24A and 24B defined by projections on the upper surface 22. In various embodiments, the frame 12 can be a one-piece, integral, monolithic structure. In various embodiments, the frame 12 can be made of a generally rigid material. The frame 12 can be made of a plastic or polymeric material, a metal, or a composite thereof. The frame 12 can be generally rectangular or square, or the frame 12 can be a rounded shape or a site-specific shape. For example, the lower surface 20 can be curved to conform to the desired bone 16. The frame 12 can be of a sufficient length to span across a region of both fragments 18 and 18′. The frame 12 can also span the entirety of the fractured area of the bone 16 and cover healthy adjacent bone 16, or the frame can be smaller than the fractured area of the bone 16. The frame 12 can also be elongated such that it spans beyond the length of the fracture or weakened area, such as the frames 12 shown in FIGS. 3 and 4.

The frame lower surface 20 can include a flat surface or the lower surface 20 can be curved to accommodate the contour of the bone 16. The upper surface 22 of the frame 12 partially defines the openings 26A and 26B for the flexible member holders 24A and 24B, respectively. The flexible member holders 24A and 24B can be channels, a post, a pin, a hole, or other means by which to retain a flexible member on the frame 12. It is understood that the flexible member holders 24A and 24B need not be formed on the upper surface 22 and that the flexible member holders 24A and 24B can extend from the lower surface 20 and around the upper surface 22. As shown in FIGS. 4 and 8, the frame 12 can include a plurality of flexible member holders 24A-24D which can be separated by a space 28 between the sets of flexible member holders 24C and 24A, and 24D and 24B. Although various embodiments disclosed may relate to only two flexible member holders, it is understood that the processes of use are generally the same for assemblies having 2 through 8, or more flexible member holders.

Any of the flexible member holders 24A-24D can be open such that the adjustable flexible member construct 14 can be repeatedly manually placed and removed, or the flexible member holders 24A-24D can be closed such that the adjustable flexible member construct 14 is permanently housed therein and cannot be inadvertently removed without disassembling the adjustable flexible member construct 14. The flexible member holders 24A-240 can be sized to allow the adjustable flexible member construct 14 to freely slide therein. The flexible member holders 24A-24D can be pre-formed to be closed or can be initially provided as an open and subsequently crimped or pinched closed. FIG. 1 depicts the frame having an open flexible member holder 24A and a closed flexible member holder 24B while FIG. 2 depicts two open flexible member holders 24A and 24B.

In various embodiments, the flexible member holders 24A and 24B face each other or are opposed. This allows for the adjustable flexible member construct 14 to be disposed in a first flexible member holder, for example flexible member holder 24B, wrapped around the bone 16, and then be disposed in the other flexible member holder, for example flexible member holder 24A, and tightened when the flexible member construct 14 is engaged such that opposing force is applied to the opposing flexible member holder to provide compression.

As shown in FIGS. 3 through 5C and FIGS. 8 and 9, the frame 12 can define at least one opening 30 in which to attach a fastener 32 such as a pin, screw, spike, or a combination or variation thereof to bone. The frame 12 can include a plurality of fastener openings 30 to accommodate multiples of the same or different fasteners 32. The fastener openings 30 can be placed along the periphery of the frame 12 as shown in FIGS. 5A through 5C, or the fastener openings 30 can cut through the lower surface 20 and upper surface 22 of the frame 12. The fastener openings 30 can be evenly placed on or about the frame 12, as shown in FIG. 5B and FIG. 9, or they can be asymmetrically placed on or about the frame 12, as shown in FIG. 5A. It is understood that the fastener openings 30 can be placed anywhere along the frame 12 at any angle and can be placed within the interior of the frame 12.

Referring to FIG. 1, the frame 12 can be used to hold the adjustable flexible member construct 14 as depicted in FIGS. 6A and 6B. The adjustable flexible member construct 14 is fashioned from a flexible member 34 made of any biocompatible material that is flexible and can fold around and secure the bone 16. Exemplary materials include, but are not limited to, non-resorbable polymers, such as polyethylene or polyester, resorbable polymers, metals, and various combinations thereof. The materials can include those formed into a monofilament, multiple filaments, cables, and the like. In various embodiments, the adjustable flexible member construct 14 is made of a hollow material to allow for the appropriate folding and tensioning. In various embodiments, the adjustable flexible member construct 14 can be a suture. In such embodiments, the suture can be hollow or a braided or multiple-filament suture structure. In various embodiments, the adjustable flexible member construct 14 can define a substantially tubular hollow shape.

To form the adjustable flexible member construct 14, a first end 36 of the flexible member is passed through a first aperture 38 and through a longitudinal passage 40 and out a second aperture 42. A second end 44 is passed through the second aperture 42, through the longitudinal passage 40 and out the first aperture 38. In various embodiments, the first and second apertures 38 and 42 are formed during the braiding process as loose portions between pairs of fibers defining the flexible member 34. Passing the ends 36 and 44 through the apertures 38 and 42 forms loops 46 and 46′. The longitudinal and parallel placement and advancement of the first and second ends 36 and 44 of the flexible member 34 within the longitudinal passage 40 resists the reverse relative movement of the first and second portions 48 and 50 of the flexible member 34 once it is tightened. A further discussion of the flexible member construct is provided in U.S. patent Ser. No. 11/541,506 filed on Sep. 29, 2006 entitled “Method And Apparatus For Forming A Self-Locking Adjustable Suture Loop” assigned to Biomet Sports Medicine, Inc., and the disclosure is incorporated by reference.

The loops 46 and 46′ define mounts or summits 52 and 52′ of the adjustable flexible member construct 14 and are disposed opposite from the longitudinal passage 40 such that when the summit 52 is disposed in a first flexible member holder 24A and the longitudinal passage 40 is disposed in a second flexible member holder 24B, the summit 52 and the longitudinal passage 40 remain stationary with respect to the frame 12, while the overall diameter of the adjustable flexible member construct 14 is decreased to compress the bone fragments 18 and 18′.

The tensioning of the ends 36 and 44 cause relative translation of the sides of the flexible member 34 with respect to each other. Upon applying tension to the first and second ends 36 and 44 of the flexible member 34, the size of the loop(s) 46 is reduced to a desired size or load. The flexible member 34 locks without knots due to the tensioning placed on the first and second ends 36 and 44. At this point, additional tension causes the body of the flexible member defining the longitudinal passage 40 to constrict about the portions 48 and 50 of the flexible members within the longitudinal passage 40. This constriction reduces the diameter of the longitudinal passage 40, thus forming a mechanical interface between the exterior surfaces of the first and second portions 48 and 50, as well as the interior surface of the longitudinal passage 40. This constriction causes the adjustable flexible member to “automatically” lock in a reduced or smaller diameter position.

In use, the assembly 10 is formed by coupling the adjustable flexible member construct 14 to the frame 12. The lower surface 20 is placed such that it abuts the bone fragments 18 and 18′. In embodiments where at least one flexible member holder 24A or 24B is closed, the summit 52 is placed in the open flexible member holder 24B opposite the longitudinal passage 40 disposed in the opposing closed flexible member holder 24A. The flexible member free ends 36 and 44 are engaged and pulled in the direction of the arrow shown in FIG. 7 such that the diameter of the loop 46 is reduced and the bone fragments 18 and 18′ are compressed. In embodiments where the longitudinal passage 40 is not pre-disposed in the closed flexible member holder 24A or where both flexible member holders are open, the longitudinal passage 40 and the summit 52 are placed in the respective, opposing flexible member holder and then the free ends 36 and 44 are engaged to tighten the adjustable flexible member construct 14 and secure the bone fragments 18 and 18′. No additional steps, such as knot tying, are required to secure the adjustable flexible member due to the automatic locking feature.

Turning to FIGS. 10A through 15C, in still other embodiments, an assembly 110 is provided. The assembly 110 shares several similarities with the assembly 10 detailed above. It is understood that the assembly 110 and the assembly 10 can have interchangeable features and the discussion of separate features on the respective assemblies is not intended to be a limitation of the present teachings.

The assembly 110 includes a frame or fixation plate 112 and an adjustable flexible member construct 114. The frame 112 includes a lower surface 120, an upper surface 122, and at least one flexible member holder, depicted as a post 124, thereon about which the adjustable flexible member construct 114 can be secured.

The post 124 sits proud to the upper surface 122 of the frame. The post 124 can be centered on the frame 112, or the post 124 can be placed at an off-center point on the frame 112. The post 124 can be generally smooth and cylindrical as shown in FIGS. 10A and 10B, or the post 124 can be a squared or have any other suitable geometry. The post 124 can include surface features by which the adjustable flexible member construct 114 can be disposed in or through, such as a notch, under cut, groove, or throughbore. An exemplary under cut or notch 126 is shown in FIG. 10A.

The frame 112 can have a flat profile or the frame 112 can have a slightly curved profile, such as those shown in FIGS. 10A and 10B, respectively. As shown in FIG. 12, for example, the frame 112 can define openings 130 to receive fasteners 132 such as those detailed earlier herein. Although a plurality of evenly spaced fastener openings 130 are depicted on the frame 112 in FIG. 12, it is understood that the fastener openings 130 can be placed anywhere along the periphery of the frame 112, can be placed through the center of the post 124, or can be asymmetrically placed. The fastener openings 130 can also be threaded to receive screws. In various embodiments, the fastener openings 130 can include both machine threads and bone engaging threads.

In use, the lower surface of the frame 112 is placed against the bone fragments 18 and 18′. Either of the summit 52 or the longitudinal passage 40 of the adjustable flexible member construct 14 is disposed about the post 124. The other of the summit 52 or the longitudinal passage 40 is partially circled about the bone 16 and is disposed on the opposite side of the post 124. In embodiments where the post 124 includes the notch 126, the adjustable flexible member construct 14 can be disposed in the notch 126 during the wrapping process. The ends 36 and 44 of the adjustable flexible member construct 14 are engaged to reduce the diameter of the adjustable flexible member construct 14 about the bone 16 and thereby compress the bone fragments 18 and 18′.

Turning to FIGS. 15A-15D, in various embodiments, the assembly 210 can include an upper fixation element 200 and a lower fixation element 202 having the adjustable flexible member construct 14 spanning therebetween through an opening 204 formed in the bone fragments 18 and 18′. The upper fixation element 200 and lower fixation element 202 can independently be selected from a grommet 206, a toggle 208, a button 209, a screw tip 212, a screw head 214, a set screw head 216, or other similar items. The screw elements (e.g., the screw tip 212, the screw head 214, and the set screw head 216) may be provided with self-tapping threads to omit the need for an additional tapping operation. As with the frame 12, the assembly 210 can be made of a generally rigid material, such as a plastic or polymeric material, a metal, or a composite thereof. Any of the elements of the assembly 210 can also be formed from a porous material for bony ingrowth. In any embodiment, however, the material of the assembly 210 should be formed from a biocompatible material.

As shown in FIG. 15A, the upper fixation element 200 is the grommet 206 and the lower fixation element is the toggle 208. The toggle 208 is used to hold the longitudinal passage 40 of the adjustable flexible member construct 14 and the opposing region is contained by the grommet 206 in bone fragment 18. The adjusting arms 36 and 44 are also passed through the grommet 206 and can be pulled to tighten the adjustable flexible member construct 14 and compress the bone fragments 18 and 18′ together. In particular, the grommet 206 may define a loop portion 218 and a central cavity 220. The summit 52 may be disposed in the loop portion 218 opposite the longitudinal passage 40 disposed in the opposing toggle 208. The ends 36, 44 may pass on either side of the loop portion 218 and extend through the central cavity 220. In operation, the ends 36, 44 may be engaged and pulled in the upward/outward direction such that the diameter of the loop 46 is reduced and the bone fragments 18 and 18′ are compressed so as to be self-locking. While the adjustable flexible member construct 14 is shown and described as a single loop construct (FIG. 6A), it should also be understood that adjustable flexible member construct 14 may have a double loop construct (FIG. 6B).

The upper fixation element 200 and lower fixation element 202 are shown in connection with the fixation plate 112 where the grommet 206 is disposed in the opening 130 in the fixation plate 112. It is understood that the plate 112 can be used with either of the upper fixation element 200 or the lower fixation element 202. When used with the grommet 206, however, a portion of the bone fragment 18′ may be reamed so as to provide a countersink 222 for receipt of at least the loop portion 218. In particular, the countersink 222 may be sized so as to allow a top surface 224 of the grommet 206 to lie flush with a top surface 226 of the fixation plate 112 after tightening.

FIGS. 15B, 15C, and 15D depict assemblies without the fixation plate 112 shown in FIG. 15A. Similar to the previously discussed embodiment, an opening 204 is prepared in the bone fragments 18 and 18′. The opening 204 is a partial opening and does not extend all of the way through both bone fragments 18 and 18′.

With specific reference to FIG. 15B, the button 209 is used as the upper fixation element 200 and the screw tip 212 serves as the lower fixation element 202. The lower fixation element 202 (i.e., the screw tip 212) may have an eyelet structure 228 for retaining the longitudinal passage 40 of the adjustable flexible member construct 14. The screw tip 212 may be fixed into the bone fragment 18. At least the free ends 36 and 44 and the summit 52 of the adjustable flexible member construct 14 are disposed through the button 209, through lacing for example, and can be adjusted to provide the secured fit and bone fragment 18 and 18′ fixation. In particular, the ends 36, 44 may be engaged and pulled in the upward/outward direction such that the diameter of the loop 46 is reduced and the bone fragments 18 and 18′ are maintained in a compressed position. While the adjustable flexible member construct 14 is shown and described as a single loop construct (FIG. 6A), it should also be understood that adjustable flexible member construct 14 may have a double loop construct (FIG. 6B). In such a case, the summit 52′ may extend through the same holes as the summit 52. Furthermore, while the button 209 is shown as having a 4-hole arrangement, it is also contemplated that only 2 holes may be present. In a 2-hole arrangement, both summits 52, 52′ and the ends 36, 44 may extend through the same holes.

Turning to FIG. 15C, the upper fixation element 200 is depicted as the telescoping screw head 214, and the lower fixation element 202 as the screw tip 212. The screw tip 212 may be fixed in the bone fragment 18 for retaining the longitudinal passage 40 of the adjustable flexible member construct 14, as described above. A sleeve member 230 may be located between the upper and lower fixation elements 200, 202 so as provide a telescoping arrangement for the screw head 214. The sleeve member 230 may be an individual element or may be integrally formed with the screw tip 212. The telescoping screw head 214 may have a cross drilled hole 232 for receiving the summit 52 and a central aperture 234 for receiving the adjustable free ends 36 and 44 of the adjustable flexible member construct 14. When tightening the adjustable flexible member construct 14 as previously described, the telescoping screw head 214 can be aligned with the sleeve member 230 and can be compressed towards the distally placed screw tip 212 to secure the fracture. The sleeve member 230 prevents side movement of the screw head 214 during tightening and compression of the fracture.

With reference now to FIG. 15D, the upper fixation element 200 of the assembly 210 is depicted as the set screw head 216 either flush with or inset below an outer surface of the bone fragment 18′, while the lower fixation element 202 is depicted again as the screw tip 212. The set screw head 216 may be provided with a female sleeve 236 extending within the bone fragment 18′, while the screw tip 212 may be provided with the sleeve member 230 extending within the bone fragment 18. In this way, the male sleeve 230 of the screw tip 212 may be telescopically received within the female sleeve 236 of the set screw head 216.

It should be understood that sleeves 230, 236 may be either integrally formed or separately formed and later secured to the set screw head 216 or screw tip 212, respectively. It should also be understood that the male-female telescoping arrangement may be reversed so as to provide the male portion at the set screw head 216 and the female portion at the screw tip 212. Additionally, the set screw head 216 and screw tip 212 may each have an external screw thread wherein the outer thread diameters may be similar, as shown, or may be provided with different diameter profiles to accommodate a particular fracture zone (e.g., the outer diameter of the set screw head 216 may be greater than the outer diameter of the screw tip 212). With either outer diameter arrangement, the assembly 210 is fixed in the bone fragments 18 and 18′ such that the upper fixation element 200 is secured within the bone fragment 18′ and the lower fixation element 202 is secured within the bone fragment 18, as will be described in more detail below with respect to FIGS. 17A-17D.

The adjustable flexible member construct 14 may extend between the upper and lower fixation elements 200, 202, as described above. In particular, the adjustable flexible member construct 14 may have the longitudinal passage 40 passing through the eyelet structure 228 of the screw tip 212, while at least the summits 52, 52′ may pass through a central plate 234 in the set screw head 216. For example, the central plate 234 may have a plurality of apertures 238 for receiving at least the summits 52, 52′ and ends 36, 44, as shown. For example, the ends 36, 44 may pass through a first pair of apertures 240, while the summits 52, 52′ may pass through a second pair of apertures 242 in the set screw head 216, as shown in FIG. 15E. Conversely, the ends 36, 44 and the summits 52, 52′ may commonly pass through the first pair of apertures 240 of the set screw head 216, as best shown in FIG. 15F. While described as having a central plate 234, it should be understood that any arrangement for receiving the summits 52, 52′ and ends 36, 44 may be appropriate. For example, the upper fixation element 200 may have a solid body with at least two apertures extending therethrough or the upper fixation element may have an enlarged upper bore with a plate-like piece inserted therein for retaining the summits 52, 52′.

As previously described, the ends 36, 44 may be engaged and pulled in the upward/outward direction such that the diameter of the loop 46 is reduced and the bone fragments 18 and 18′ are compressed. The ends 36, 44 may be tied so as to resist the reverse relative movement of the first and second portions 48 and 50 of the flexible member 34 once it is tightened. While the adjustable flexible member construct 14 is shown as described with reference to FIG. 6B, other constructs may be used in combination with the upper and lower fixation elements 200, 202 such as those described in U.S. Pat. No. 7,601,165 to Stone, issued Oct. 13, 2009, and is incorporated by reference in its entirety herein.

With reference now to FIGS. 15E and 15F, the female sleeve 236 may have an internally keyed surface 244 corresponding to an externally keyed surface 246 of the male sleeve 230. For example, the externally keyed surface 246 of the male sleeve 230 may be in the shape of a protrusion 248 (FIG. 15E) or may be in the shape of a polygon, such as a hexagonal arrangement 250 (FIG. 15F). In this way, both the upper and lower fixation elements 200, 202 may be rotationally driven at the same time. In particular, a hexagonal driver (not shown) may be inserted into a non-cylindrical or faceted upper drive bore 252 in the set screw head 216. The hexagonal driver may provide a torque for rotation the set screw head 216 into the bone fragment 18′, while the mated internally keyed surface 244 and the externally keyed surface 246 may rotate the screw tip 212 through the bone fragment 18′ and into the bone fragment 18 simultaneously. Alternatively, the upper and lower fixation elements 200, 202 may be separately driven into the bone fragments 18, 18′.

The present teachings further provide methods for securing the fractured or weakened bone 16 within a patient's body. The frame 12 is abutted against the fractured or weakened bone 16 such that the lower surface 20 sits against the bone. The frame 12 can be positioned to span across both sides of the fracture. The summit 52 or the longitudinal passage 40 is disposed in one of the flexible member holders 24A or 24B defined by the frame 12. The fractured or weakened bone 16 is then encircled by partially wrapping the adjustable flexible member construct 14 at least partially contained in the frame about the bone. The other of the summit 52 or the longitudinal passage 40 is fixed in the second, opposing flexible member holder 24B. In embodiments where a plurality of frames 12 or the plurality of flexible member holders 24A-24D are provided on the frame 12, the process can be repeated by employing several adjustable flexible member constructs 14 in various sets of flexible member holders, for example the set 24A/24C and the set 24B/24D of FIG. 4 and FIG. 8. The process can also be repeated by wrapping a single adjustable flexible member construct 14 about the area to engage several flexible member holders on the different frames, such as where the frames are used in tandem across a fractured or weakened bone.

The ends 36 and 44 of the adjustable flexible member construct 14 are engaged or pulled to reduce the size of the loop 46 and to cause the summit 52 and the longitudinal passage to press against the respective opposed flexible member holders. This compresses the bone fragments 18 and 18′ at the compromised site. In embodiments where the frame 12 is made of a rigid material, engaging the free ends 36 and 44 does not cause the frame 12 to stretch, lengthen, or otherwise increase in size, thereby allowing for tighter compression. In embodiments utilizing fasteners 32 or 132, the fasteners can be secured to the bone fragments, 18 and 18′ before or after the adjustable flexible member construct 14 is reduced about the bone 16. The flexible member constructs allow additional tensioning of each individual flexible member construct independently, so as to avoid any laxity that may occur to a flexible member construct as others are tightened.

In still further embodiments such as those shown in FIGS. 16A and 16B, the frame 112 can be attached via a pedicle screw 134 which is affixed to vertebra 136. The pedicle screw 134 is passed through the fastener opening 130 which is defined by the post 124. The pedicle screws 134 can be linked together using the adjustable flexible member construct 14. As shown in FIG. 16B, a single adjustable flexible member construct 14 can be attached to two or more assemblies 10. Alternatively, as shown in FIGS. 16A and 16B, multiple adjustable flexible member constructs 14 can be attached to one or more pedicle screws 134.

With reference now to FIGS. 17A-17D, a method for securing a fractured bone using the assembly 210 shown in FIG. 15D, is described. In particular as shown in FIG. 17A, an aimer (not shown) may be used to guide a guide wire 260 through a selected portion of the fractured bone 16. Appropriate aimers are generally known and need not be described in detail herein. Also, other techniques for placing the guide wire 260 in the fractured bone 16 are also generally known and not described in detail herein. For example, such a device and method is described in U.S. Pat. No. 7,736,364, Stone, issued Jun. 15, 2010, and is incorporated by reference in its entirety herein. It will also be understood that the procedure may be augmented with an arthroscope (not shown) that may be passed through an appropriate incision in the soft tissue surrounding the fractured bone 16.

After removal of the aimer, a longitudinal bore 262 of a cannulated bone cutting tool (e.g., drill 264) may be placed over the guide wire 260 to guide the bone cutting tool 264 as it is brought into engagement with the fractured bone 16, as shown in FIG. 17B. The bone cutting tool 264 may be used to drill an aperture 266 within at least a portion of the fractured bone 16. For example, the bone cutting tool 264 may drill through the bone fragment 18′ and into a portion of the bone fragment 18. The guide wire 260 may then be removed from the fractured bone 16.

With reference now to FIG. 17C, the assembly 210 may be inserted into the aperture 266. In particular, a driver (not shown) may be inserted into the upper drive bore 252 of the set screw head 216 for rotation therewith. Rotation of the set screw head 216, in turn, provides a torque to the screw tip 212 through the keyed surfaces 244, 246, causing it to translate through the bone fragment 18′ and into the bone fragment 18, as previously described. Notably, the assembly 210 may be pre-assembled such that the longitudinal passage 40 of the adjustable flexible member construct 14 is passed through the eyelet structure 228 of the lower fixation element 202, at least one summit 52 or 52′ of the adjustable flexible member construct 14 is passed through the upper fixation element 200, and the ends 36, 44 of the adjustable flexible member construct 14 extend through the corresponding loop portion 238 in the upper fixation element 200.

Referring now to FIG. 17D, the adjustable flexible member construct 14 may then be reduced for compressing the fractured bone 16. In particular, the ends 36, 44 of the adjustable flexible member construct 14 may be engaged such that a distance between the upper and lower fixation elements 200, 202 is decreased and the adjustable flexible member construct 14 automatically remains in a reduced position within the fractured bone 16. During this reduction, the male sleeve member 230 of the lower fixation element 202 is telescopically received within the female sleeve member 236 of the upper fixation element 200.

The description of the invention is merely exemplary in nature and, thus, variations that do not depart from the gist of the invention are intended to be within the scope of the invention. For example, any of the above mentioned surgical procedures is applicable to the repair of other body portions. For example, the procedures can be equally applied to orthopedic repair of wrists, fingers, legs, ankles, and other bones and also to non-orthopedic repairs. Such variations are not to be regarded as a departure from the spirit and scope of the invention. 

What is claimed is:
 1. A bone compression assembly, comprising: a first fixation element securable in a first bone portion; a second fixation element securable in a second bone portion; and an adjustable suture construct extending between the first fixation element and the second fixation element, the adjustable suture construct including a suture with a free end that extends longitudinally through a longitudinal passage in the suture to form an adjustable loop, wherein the adjustable suture construct is coupled to the first fixation element and the second fixation element such that, with the free end extending longitudinally through the longitudinal passage in the suture to form the adjustable loop, the free end can be pulled through the longitudinal passage to decrease a size of the adjustable loop for pulling the first fixation element and the second fixation element toward one another, wherein the first fixation element and the second fixation element each include external threading and are matable together via a keyed arrangement between the first fixation element and the second fixation element such that the first fixation element and the second fixation element can be simultaneously rotationally driven through bone.
 2. The bone compression assembly of claim 1, wherein the free end is a first free end, the longitudinal passage is a first longitudinal passage, and the adjustable loop is a first adjustable loop, the suture further including a second free end that extends longitudinally through a second longitudinal passage in the suture to form a second adjustable loop.
 3. The bone compression assembly of claim 2, wherein, with the first free end extending longitudinally through the first longitudinal passage in the suture to form the first adjustable loop and with the second free end extending longitudinally through the second longitudinal passage in the suture to form the second adjustable loop, the first free end can be pulled through the first longitudinal passage to decrease the size of the first adjustable loop without decreasing a size of the second adjustable loop and the second free end can be pulled through the second longitudinal passage to decrease the size of the second adjustable loop without decreasing the size of the first adjustable loop.
 4. The bone compression assembly of claim 2, wherein the first longitudinal passage is separate from the second longitudinal passage in the suture.
 5. The bone compression assembly of claim 2, wherein the first free end extends into the suture through a first aperture in the suture, longitudinally within the suture along the first longitudinal passage, and out of the suture through a fourth aperture in the suture to form the first adjustable loop, and wherein the second free end extends into the suture through a second aperture in the suture, longitudinally within the suture along the second longitudinal passage, and out of the suture through a third aperture in the suture to form the second adjustable loop, the first aperture, the second aperture, the third aperture, and the fourth aperture all being separate apertures in the suture.
 6. The bone compression assembly of claim 5, wherein, with the first free end extending into the suture through the first aperture in the suture, longitudinally within the suture along the first longitudinal passage, and out of the suture through the fourth aperture in the suture to form the first adjustable loop and with the second free end extending into the suture through the second aperture in the suture, longitudinally within the suture along the second longitudinal passage, and out of the suture through the third aperture in the suture to form the second adjustable loop, the first free end can be pulled through the first longitudinal passage to decrease a size of the first adjustable loop without decreasing a size of the second adjustable loop and the second free end can be pulled through the second longitudinal passage to decrease a size of the second adjustable loop without decreasing a size of the first adjustable loop.
 7. The bone compression assembly of claim 1, wherein the first fixation element includes at least a first hole, a second hole, and a third hole with a summit of the adjustable suture construct passing through the first hole and the second hole and with the free end of the adjustable suture construct passing through the third hole.
 8. A bone compression assembly, comprising: a first fixation element securable in a first bone portion; a second fixation element securable in a second bone portion; and an adjustable suture construct including a suture with a free end that extends longitudinally through a longitudinal passage in the suture to form an adjustable loop, wherein the first fixation element is coupled to the second fixation element with the adjustable suture construct such that, with the free end extending longitudinally through the longitudinal passage in the suture to form the adjustable loop, the free end can be pulled through the longitudinal passage to decrease a size of the adjustable loop for pulling the first fixation element and the second fixation element toward one another, the first fixation element including a first sleeve member through which the adjustable suture construct extends to couple the first fixation element to the second fixation element, the second fixation element including a second sleeve member through which the adjustable suture construct extends to couple the first fixation element to the second fixation element, the first sleeve member and the second sleeve member being matable together via a keyed arrangement between the first sleeve member and the second sleeve member such that the first fixation element and the second fixation element can be simultaneously rotationally driven through bone.
 9. The bone compression assembly of claim 8, wherein the free end is a first free end, the longitudinal passage is a first longitudinal passage, and the adjustable loop is a first adjustable loop, the suture further including a second free end that extends longitudinally through a second longitudinal passage in the suture to form a second adjustable loop.
 10. The bone compression assembly of claim 9, wherein, with the first free end extending longitudinally through the first longitudinal passage in the suture to form the first adjustable loop and with the second free end extending longitudinally through the second longitudinal passage in the suture to form the second adjustable loop, the first free end can be pulled through the first longitudinal passage to decrease the size of the first adjustable loop without decreasing a size of the second adjustable loop and the second free end can be pulled through the second longitudinal passage to decrease the size of the second adjustable loop without decreasing the size of the first adjustable loop.
 11. The bone compression assembly of claim 9, wherein the first longitudinal passage is separate from the second longitudinal passage in the suture.
 12. The bone compression assembly of claim 9, wherein the first free end extends into the suture through a first aperture in the suture, longitudinally within the suture along the first longitudinal passage, and out of the suture through a fourth aperture in the suture to form the first adjustable loop, and wherein the second free end extends into the suture through a second aperture in the suture, longitudinally within the suture along the second longitudinal passage, and out of the suture through a third aperture in the suture to form the second adjustable loop, the first aperture, the second aperture, the third aperture, and the fourth aperture all being separate apertures in the suture.
 13. The bone compression assembly of claim 12, wherein, with the first free end extending into the suture through the first aperture in the suture, longitudinally within the suture along the first longitudinal passage, and out of the suture through the fourth aperture in the suture to form the first adjustable loop and with the second free end extending into the suture through the second aperture in the suture, longitudinally within the suture along the second longitudinal passage, and out of the suture through the third aperture in the suture to form the second adjustable loop, the first free end can be pulled through the first longitudinal passage to decrease a size of the first adjustable loop without decreasing a size of the second adjustable loop and the second free end can be pulled through the second longitudinal passage to decrease a size of the second adjustable loop without decreasing a size of the first adjustable loop.
 14. The bone compression assembly of claim 8, wherein the first fixation element includes at least a first hole, a second hole, and a third hole with a summit of the adjustable suture construct passing through the first hole and the second hole and with the free end of the adjustable suture construct passing through the third hole.
 15. The bone compression assembly of claim 8, wherein at least one of the first fixation element and the second fixation element includes external threading.
 16. The bone compression assembly of claim 15, wherein the first fixation element and the second fixation element include external threading.
 17. A bone compression assembly, comprising: a first fixation element that includes external threading, the first fixation element securable in a first bone portion; a second fixation element that includes external threading, the second fixation element securable in a second bone portion; and an adjustable suture construct extending between the first fixation element and the second fixation element, the adjustable suture construct including a suture with a free end that extends longitudinally through a longitudinal passage in the suture to form an adjustable loop, wherein the adjustable suture construct is coupled to the first fixation element and the second fixation element such that, with the free end extending longitudinally through the longitudinal passage in the suture to form the adjustable loop, the free end can be pulled through the longitudinal passage to decrease a size of the adjustable loop for pulling the first fixation element and the second fixation element toward one another, wherein the first fixation element includes at least a first hole, a second hole, and a third hole with a summit of the adjustable suture construct passing through the first hole and the second hole and with the free end of the adjustable suture construct passing through the third hole.
 18. The bone compression assembly of claim 17, wherein the free end is a first free end, the longitudinal passage is a first longitudinal passage; and the adjustable loop is a first adjustable loop, the suture further including a second free end that extends longitudinally through a second longitudinal passage in the suture to form a second adjustable loop.
 19. The bone compression assembly of claim 18, wherein the second free end passes through a fourth hole in the first fixation element.
 20. The bone compression assembly of claim 18, wherein the first longitudinal passage is separate from the second longitudinal passage in the suture.
 21. The bone compression assembly of claim 18, wherein the first free end extends into the suture through a first aperture in the suture, longitudinally within the suture along the first longitudinal passage, and out of the suture through a fourth aperture in the suture to form the first adjustable loop, and wherein the second free end extends into the suture through a second aperture in the suture, longitudinally within the suture along the second longitudinal passage, and out of the suture through a third aperture in the suture to form the second adjustable loop, the first aperture, the second aperture, the third aperture, and the fourth aperture all being separate apertures in the suture. 